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Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing

Modifications in the tRNA anticodon loop, adjacent to the three-nucleotide anticodon, influence translation fidelity by stabilizing the tRNA to allow for accurate reading of the mRNA genetic code. One example is the N1-methylguanosine modification at guanine nucleotide 37 (m(1)G37) located in the an...

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Autores principales: Hoffer, Eric D, Hong, Samuel, Sunita, S, Maehigashi, Tatsuya, Gonzalez, Ruben L, Whitford, Paul C, Dunham, Christine M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577736/
https://www.ncbi.nlm.nih.gov/pubmed/33016876
http://dx.doi.org/10.7554/eLife.51898
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author Hoffer, Eric D
Hong, Samuel
Sunita, S
Maehigashi, Tatsuya
Gonzalez, Ruben L
Whitford, Paul C
Dunham, Christine M
author_facet Hoffer, Eric D
Hong, Samuel
Sunita, S
Maehigashi, Tatsuya
Gonzalez, Ruben L
Whitford, Paul C
Dunham, Christine M
author_sort Hoffer, Eric D
collection PubMed
description Modifications in the tRNA anticodon loop, adjacent to the three-nucleotide anticodon, influence translation fidelity by stabilizing the tRNA to allow for accurate reading of the mRNA genetic code. One example is the N1-methylguanosine modification at guanine nucleotide 37 (m(1)G37) located in the anticodon loop andimmediately adjacent to the anticodon nucleotides 34, 35, 36. The absence of m(1)G37 in tRNA(Pro) causes +1 frameshifting on polynucleotide, slippery codons. Here, we report structures of the bacterial ribosome containing tRNA(Pro) bound to either cognate or slippery codons to determine how the m(1)G37 modification prevents mRNA frameshifting. The structures reveal that certain codon–anticodon contexts and the lack of m(1)G37 destabilize interactions of tRNA(Pro) with the P site of the ribosome, causing large conformational changes typically only seen during EF-G-mediated translocation of the mRNA-tRNA pairs. These studies provide molecular insights into how m(1)G37 stabilizes the interactions of tRNA(Pro) with the ribosome in the context of a slippery mRNA codon.
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spelling pubmed-75777362020-10-23 Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing Hoffer, Eric D Hong, Samuel Sunita, S Maehigashi, Tatsuya Gonzalez, Ruben L Whitford, Paul C Dunham, Christine M eLife Biochemistry and Chemical Biology Modifications in the tRNA anticodon loop, adjacent to the three-nucleotide anticodon, influence translation fidelity by stabilizing the tRNA to allow for accurate reading of the mRNA genetic code. One example is the N1-methylguanosine modification at guanine nucleotide 37 (m(1)G37) located in the anticodon loop andimmediately adjacent to the anticodon nucleotides 34, 35, 36. The absence of m(1)G37 in tRNA(Pro) causes +1 frameshifting on polynucleotide, slippery codons. Here, we report structures of the bacterial ribosome containing tRNA(Pro) bound to either cognate or slippery codons to determine how the m(1)G37 modification prevents mRNA frameshifting. The structures reveal that certain codon–anticodon contexts and the lack of m(1)G37 destabilize interactions of tRNA(Pro) with the P site of the ribosome, causing large conformational changes typically only seen during EF-G-mediated translocation of the mRNA-tRNA pairs. These studies provide molecular insights into how m(1)G37 stabilizes the interactions of tRNA(Pro) with the ribosome in the context of a slippery mRNA codon. eLife Sciences Publications, Ltd 2020-10-05 /pmc/articles/PMC7577736/ /pubmed/33016876 http://dx.doi.org/10.7554/eLife.51898 Text en © 2020, Hoffer et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biochemistry and Chemical Biology
Hoffer, Eric D
Hong, Samuel
Sunita, S
Maehigashi, Tatsuya
Gonzalez, Ruben L
Whitford, Paul C
Dunham, Christine M
Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing
title Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing
title_full Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing
title_fullStr Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing
title_full_unstemmed Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing
title_short Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing
title_sort structural insights into mrna reading frame regulation by trna modification and slippery codon–anticodon pairing
topic Biochemistry and Chemical Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577736/
https://www.ncbi.nlm.nih.gov/pubmed/33016876
http://dx.doi.org/10.7554/eLife.51898
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